Quality Inspector I
About The Position
At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care). Position Summary: The Quality Inspector I will be responsible for raw material sampling and inspection internally and at a third-party warehouse. This individual will also be responsible for overseeing the inventory of laboratory chemicals and critical reagent supplies across both the Cambridge and Burlington facilities. Schedule: This position is in-office Monday-Friday and will require travel between Cambridge, Burlington MA, and warehouse locations regularly (~50%).
Requirements
- HS Diploma, 0-1 years’ industry experience in cGMP, or equivalent.
- Direct work experience in raw materials quality inspection system and related systems.
- Effective time management, multitasking and organizational skills.
- Strong attention to detail and cross functional team experience.
- Must be able to lift/pull up to 40 pounds.
- Personal transportation required.
- Occasional Weekend or Holiday coverage (as needed).
- Rotating off-shift alarm coverage. May be required to carry a company issued cell phone
Nice To Haves
- Direct technical experience writing CAPA’s.
- Computer skills in systems such as Microsoft Word, Excel and TrackWise.
- Knowledge of Laboratory Information Management Systems (LIMS).
Responsibilities
- Perform inspection, sampling, testing, and disposition of components and raw materials as per SOP's and specifications.
- Collaborate regularly with R&D, QA and Materials Management.
- Partner with outside vendors to coordinate offsite QC operations.
- Support of Quality Control operations by performing basic laboratory responsibilities including environmental monitoring, lab support, inventory of laboratory chemicals and critical reagent supplies, and sample submissions to contract labs.
- Create, revise, issue material specifications.
- Individual will facilitate and monitor the material lifecycle process.
- Flexible and responsive to customer needs.
- Other responsibilities as required.
Benefits
- Cutting-Edge Science: Work with a leading regenerative medicine product that is transforming patient care.
- Career Growth: Be a part of a growing organization with opportunities to expand your impact.
- Collaborative Culture: Work alongside a team of dedicated professionals who are passionate about improving lives.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
Number of Employees
251-500 employees
